Protease Inhibitors

(S,R,S)-AHPC-C5-COOH (VH032-C5-COOH) is a synthesized E3 ligase ligand-linker conjugate , contains the VH032 VHL-based ligand and a linker to form PROTAC s. VH-032 is a selective and potent inhibitor of VHL/HIF-1α interaction with a K d of 185 nM,

(S,R,S)-AHPC-C5-COOH (VH032-C5-COOH) is a synthesized E3 ligase ligand-linker conjugate , contains the VH032 VHL-based ligand and a linker to form PROTAC s. VH-032 is a selective and potent inhibitor of VHL/HIF-1α interaction with a K d of 185 nM,

(S,R,S)-AHPC-C5-COOH (VH032-C5-COOH) is a synthesized E3 ligase ligand-linker conjugate , contains the VH032 VHL-based ligand and a linker to form PROTAC s. VH-032 is a selective and potent inhibitor of VHL/HIF-1α interaction with a K d of 185 nM,

DescriptionProtein degrader builiding block (S,R,S)-AHPC-PEG4-Azide enables the synthesis of molecules fortargeted protein degradation andPROTAC (proteolysis-targeting chimeras) technology. This conjugate contains a von Hippel–Lindau

DescriptionProtein degrader builiding block (S,R,S)-AHPC-PEG6-Azide enables the synthesis of molecules fortargeted protein degradation andPROTAC (proteolysis-targeting chimeras) technology. This conjugate contains a von Hippel–Lindau

Description(tBu)2PPh Pd G4 is a powerful ligand for classic cross-coupling reactions combined with theBuchwaldFourth Generation Palladacycle. Bench stable, soluble in most organic solvents.

Description(tBu)2PPh Pd G4 is a powerful ligand for classic cross-coupling reactions combined with theBuchwaldFourth Generation Palladacycle. Bench stable, soluble in most organic solvents.

General description：1-(2-Aminoethyl)piperidine on [1+1] condensation reaction with 3-methoxy salicylaldehyde yields tridentate Schiff base ligand.application：Reactant for synthesis of:Analogs of anticancer agentsInhibitor of Botulinum Neurotoxin

General description：1-(2-Aminoethyl)piperidine on [1+1] condensation reaction with 3-methoxy salicylaldehyde yields tridentate Schiff base ligand.application：Reactant for synthesis of:Analogs of anticancer agentsInhibitor of Botulinum Neurotoxin

General description：1-(2-Aminoethyl)piperidine on [1+1] condensation reaction with 3-methoxy salicylaldehyde yields tridentate Schiff base ligand.application：Reactant for synthesis of:Analogs of anticancer agentsInhibitor of Botulinum Neurotoxin

General description：1-(2-Aminoethyl)piperidine on [1+1] condensation reaction with 3-methoxy salicylaldehyde yields tridentate Schiff base ligand.application：Reactant for synthesis of:Analogs of anticancer agentsInhibitor of Botulinum Neurotoxin

1-(6-(3-Hydroxypropyl)-3,4-dihydro-1,8-naphthyridin-1(2H)-yl)-2,2-dimethylpropan-1-one.